Paroxetine

Product NDC
55700-040
11-digit product format
557000040
Labeler code
55700
Product ID
55700-040_ee968a1a-c44d-4378-a593-f324512fb7f6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Paroxetine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA078406
Marketing category
ANDA
Marketing start
2009-12-03
Marketing end
0000-00-00
Substance
PAROXETINE HYDROCHLORIDE HEMIHYDRATE
Active strength
10 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
X2ELS050D8PAROXETINE HYDROCHLORIDE HEMIHYDRATE110429-35-1PAROXETINE HYDROCHLORIDE HEMIHYDRATE
41VRH5220HPAROXETINE61869-08-7Paroxetine